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{{Alagille syndrome}}
{{CMG}}
==Overview==
'''Alagille syndrome''' is a multisystem [[genetic disorder]] that affects the [[liver]], [[heart]], [[eyes]],[[face]], [[skeleton]], [[kidneys]] and [[vascular system]].
==Associated Conditions==
Alagille syndrome can be associated with [[congenital heart disease]], particularly [[Tetralogy of Fallot]].  The[[kidney]]s and [[central nervous system]] may also be affected. Cases of unilateral coronal craniosynostosis have also been described in association with this syndrome.
Alagille syndrome can be associated with [[congenital heart disease]], particularly [[Tetralogy of Fallot]].  The[[kidney]]s and [[central nervous system]] may also be affected. Cases of unilateral coronal craniosynostosis have also been described in association with this syndrome.
==References==
{{reflist|2}}
[[Category:Pediatrics]]
[[Category:Gastroenterology]]
[[Category:Genetic disorders]]
[[Category:Rare diseases]]
[[Category:Hepatology]]
[[Category:Mature chapter]]
{{WH}}
{{WS}}

Revision as of 17:33, 23 September 2011

Alagille syndrome Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Alagille syndrome is a multisystem genetic disorder that affects the liver, heart, eyes,face, skeleton, kidneys and vascular system.

Associated Conditions

Alagille syndrome can be associated with congenital heart disease, particularly Tetralogy of Fallot. Thekidneys and central nervous system may also be affected. Cases of unilateral coronal craniosynostosis have also been described in association with this syndrome.

References

Template:WH Template:WS